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The nucleation model was then used to investigate the effects of the design and operating parameters on the formed nuclei size distributions and to correlate these effects to changes of the dimensionless nuclei distribution function.
From this starting point, a Monte Carlo nucleation model that simulates full nuclei size distributions as a function of the design and operating parameters that were implemented in the dimensionless nuclei distribution function is developed.
A dimensionless nuclei distribution function which describes the effects of the design and operating parameters of the nucleation process (binder spray characteristics, the nucleation area ratio between droplets and nuclei and the powder bed velocity) on the fractional surface area coverage of nuclei on a moving powder bed is developed.
The nuclei distribution can be determined genetically by analyzing segregation pattern of centromere-linked markers of spore segregants extracted from the linear asci.
This difference results from two different types of nuclei distribution in a species-specific manner after second nuclear division in meiosis within the ascus.
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In contrast, muscle histology from wild-type littermates did not show such changes in nuclei distributions.
The other differences were in the nuclei distributions, as shown in Figure 2, which are difficult to see in Figure 3 because of the darker staining.
In the case where breakage occurs the model for secondary nuclei size distribution is proposed.
Human tenocytes cultured on the crimped fibers exhibited the aligned morphology with a broader and controllable nuclei angle distribution, as compared to those on the straight fibers.
Qualitative comparison of model simulations and experimental nucleation data showed similar shapes of the nuclei size distributions.
Model simulations also showed that it is possible to predict nuclei size distributions beyond the drop controlled nucleation regime in Hapgood's nucleation regime map.
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